Dual-Defect Modified 2D/2D TiO2/g-C3N4 Heterojunction for Photocatalytic H2 Production

被引:2
作者
Wang, Jiahui [1 ]
Li, Li [1 ]
Ye, Xiangju [2 ]
Yang, Yang [3 ]
Ren, Wei [1 ]
Ge, Jingbiao [1 ]
Zhang, Sujuan [1 ]
Zheng, Xiuzhen [1 ]
Chen, Shifu [1 ]
机构
[1] Huaibei Normal Univ, Key Lab Green & Precise Synthet Chem & Applicat, Minist Educ, Huaibei 235000, Anhui, Peoples R China
[2] Anhui Sci & Technol Univ, Coll Chem & Mat Engn, Bengbu 233000, Anhui, Peoples R China
[3] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Peoples R China
基金
中国国家自然科学基金;
关键词
Z-SCHEME; TIO2; ZN0.5CD0.5S; EVOLUTION; HETEROSTRUCTURE; HYDROCHLORIDE; NANOPARTICLES; DEGRADATION; FABRICATION; VACANCIES;
D O I
10.1021/acs.cgd.4c00826
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In order to solve the current energy and environmental crisis, the design of efficient catalyst materials is a highly effective solution. In this paper, the photocatalytic performance of TiO2/g-C3N4 composites was improved by regulating their microstructure, such as by constructing nanosheet structures, defect sites, and contact interfaces. Although TiO2 had limited activity in H-2 production under visible light irradiation, it could serve as an electron acceptor of g-C3N4, and it greatly increased the photocatalytic activity of g-C3N4. The optimal TiO2/g-C3N4 composite showed good photocatalytic performance (436.3 mu mol h(-1) g(-1)), which was 23.8 and 3 times that of T400 and g-C3N4, respectively. The increased photocatalytic activity of the TiO2/g-C3N4 composite could be attributed to the higher separation rate of the photogenerated charge carriers (PCCs), more active sites for the reaction, and a lower energy barrier than that of g-C3N4. Through many characterization and testing technologies, this work deeply studies the relationship between the fine structure and reaction mechanism of 2D/2D TiO2/g-C3N4, providing a new direction and understanding for the design and development of 2D materials with highly efficient activity.
引用
收藏
页码:7605 / 7616
页数:12
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